CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS

CAMLOG IMPLANT SYSTEM MODIFIED IMPLANTS AND ABUTMENTS is an FDA 510(k)-cleared medical device (K083496) manufactured by Altatec GmbH. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 29, 2009. Regulation: 8.